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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178242Generated: November 4, 2026

7-chloro-3-(piperidin-4-yl)-1H-indole → HCID 131724872, compound

https://huagongshe.com/reaction/1178242

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-chloro-3-(piperidin-4-yl)-1H-indoleHCID 12072036—
ReactantHCID 22484004HCID 22484004—
ProductHCID 131724872HCID 131724872—

Reaction Steps

from 7-chloro-3-(piperidin-4-yl)-1H-indole and 3-bromo-1-(3,4-dihydro-1H-isoquinolin-2-yl)propan-1-one. 1H NMR (DMSO-d6): 2.05-2.25 (m, 4H); 2.80 (t, 0.8H); 2.95 (t, 1.2H); 3.00-3.20 (m, 5H); 3.30-3.45 (m, 2H); 3.55-3.65 (m, 2H); 3.65-3.75 (m, 2H); 4.65 (s, 1.2H); 4.75 (s, 0.8H); 7.00 (t, 1H); 7.15-7.25 (m, 6H); 7.70 (d, 1H); 10.70 (broad s, 1H); 11.30 (s, 1H). MS m/z: 422 (MH+), 247.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276508B2
Source datasetuspto-grants-2007_10
ORD IDord-65a4be962e2744f4bedcbd282f463863
Source noteuspto-grants-2007_10